All Articles Tagged With: "Pacemaker Recall"
Articles
Medtronic Pacemaker Recall: Kappa 600/700/900 and Sigma 100/200/300
The FDA has notified patients and cardiologists of a Medtronic pacemaker recall for approximately 21,000 Kappa and Sigma pacemakers due to a wiring defect that could cause a severe heart injury or death.
Medtronic Pacemaker Defects Reported Among Kappa and Sigma Devices
Approximately 37,000 Medtronic Kappa and Sigma pacemakers could contain a wiring defect, according to an advisory letter Medtronic sent to doctors this month. The defect could cause the pacemaker to fail and potentially result in serious injury or death.
